| NDC Code | 42023-239-01 |
|---|
| Package Description | 1 VIAL in 1 CARTON (42023-239-01) / 10 mL in 1 VIAL |
|---|
| Product NDC | 42023-239 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Methylprednisolone Acetate |
|---|
| Non-Proprietary Name | Methylprednisolone Acetate |
|---|
| Dosage Form | INJECTION, SUSPENSION |
|---|
| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE |
|---|
| Start Marketing Date | 20230512 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214297 |
|---|
| Manufacturer | Endo USA, Inc. |
|---|
| Substance Name | METHYLPREDNISOLONE ACETATE |
|---|
| Strength | 40 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|